Current partner codePEPTIDESDE
NCT00965393·Not applicable·INTERVENTIONAL

The Effect of Ischaemic-Reperfusion and Remote Ischaemic Preconditioning in Man - A Bradykinin Dependent Pathway

Status

Completed

Phase

Not applicable

Enrollment

12

Locations

1

Results

Not posted

Publications

1

Study summary

What the protocol is testing.

Heart attacks are usually caused by a blood clot blocking an artery supplying blood to the heart. Current treatments are designed at relieving this blockage as quickly as possible to minimize damage to the heart muscle. However in restoring the supply of blood local damage known as "ischaemia-reperfusion injury" may occur. The aim of this study is to assess how clot forming and clot dissolving pathways are affected during this process, and examine the role of a natural inflammatory hormone, bradykinin. This will help the investigators to understand the mechanism by which ischaemia-reperfusion injury may occur and to devise new treatments for heart attacks.

Interventions

Treatment arms and agents.

PROCEDURE

Forearm vascular study

Forearm blood flow measured by venous occlusion plethysmography during interarterial infusion of vasodilators (Ach). Venous blood sampling via cannula in antecubital fossa.

DRUG

Placebo

Systemic infusion of placebo (saline)

DRUG

bradykinin receptor antagonist (HOE-140)

Systemic infusion of bradykinin receptor antagonist (HOE-140)

Timeline

From registration to results.

  1. First posted

    Aug 25, 2009

  2. Study start

    Aug 2009

  3. Primary completion

    Oct 2010

  4. Study completion

    Oct 2010

  5. Results posted

    Not reported

  6. Registry updated

    Oct 25, 2010

Outcomes

What the study measures.

Primary outcomes

Change in forearm blood flow in response to vasodilators (ACh(, ischaemia reperfusion and ischaemic preconditioning

Time frame · 20 fixed timepoints during each study visit (3hrs)

Secondary outcomes

Change in platelet-monocyte-binding after ischaemia reperfusion and ischaemic preconditioning

Time frame · 4 fixed timepoints during each study visit (3hrs)

Eligibility

Who can take part.

Minimum age
18 Years
Maximum age
65 Years
Sex
MALE
Healthy volunteers
Yes

Inclusion Criteria: * Healthy males between 18-65 years of ages. * Non-smokers. Exclusion Criteria: * Any concurrent illness or chronic medical condition. * Concurrent use of vasoactive medication. * Smoking history.

Study locations

1 registered sites.

United Kingdom. Showing up to 24 locations stored in the fast local snapshot.

University of Edinburgh, 49 Little France Crescent

Edinburgh, United Kingdom

Related trials

More studies on Icatibant.

Related PeptideStat pages

Put the record in context.

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